Allele Registry

Canonical Allele Identifier: PA645378393

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231527

ClinVar RCV:

RCV000214442

RCV000589961

RCV000629813

RCV000708853

RCV000986701

RCV003462406

ClinVar Variation:

229725

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile120Thr	CA071457 NM_000179.3:c.359T>C